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  2. Dominance (genetics) - Wikipedia

    en.wikipedia.org/wiki/Dominance_(genetics)

    Autosomal dominant and autosomal recessive inheritance, the two most common Mendelian inheritance patterns. An autosome is any chromosome other than a sex chromosome.. In genetics, dominance is the phenomenon of one variant of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome.

  3. X-linked dominant inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_dominant_inheritance

    X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type.

  4. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    Definition Law of dominance and uniformity Some alleles are dominant while others are recessive; an organism with at least one dominant allele will display the effect of the dominant allele. [27] Law of segregation During gamete formation, the alleles for each gene segregate from each other so that each gamete carries only one allele for each gene.

  5. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    This is an accepted version of this page This is the latest accepted revision, reviewed on 27 February 2025. Science of genes, heredity, and variation in living organisms This article is about the general scientific term. For the scientific journal, see Genetics (journal). For a more accessible and less technical introduction to this topic, see Introduction to genetics. For the Meghan Trainor ...

  6. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]

  7. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.

  8. Hardy–Weinberg principle - Wikipedia

    en.wikipedia.org/wiki/Hardy–Weinberg_principle

    A dominant allele can be inherited from a homozygous dominant parent with probability 1, or from a heterozygous parent with probability 0.5. To represent this reasoning in an equation, let A t {\displaystyle \textstyle A_{t}} represent inheritance of a dominant allele from a parent.

  9. Haploinsufficiency - Wikipedia

    en.wikipedia.org/wiki/Haploinsufficiency

    The haploinsufficiency is caused by the copy-number variation (CNV) of 28 genes led by the deletion of ~1.6 Mb. These dosage-sensitive genes are vital for human language and constructive cognition. [2] Another example is the haploinsufficiency of telomerase reverse transcriptase which leads to anticipation in autosomal dominant dyskeratosis ...